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欢迎访问Eurotherm网站
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“集成合规”概念着眼于对现有系统组件进行处理以减小进行有效性验证所需作出的努力。最大限度地重用硬件以及软件使您能够将过时系统“整合”为适合的架构,以期 GxP 系统”符合”管理规范,包括 FDA 的 21 CFR 第 11 部分.
让我们来帮助您识别非兼容系统,并采取必要的补救措施以使其有效：
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